全基因组测序：全基因组范围内其他致病变异的鉴定。
Whole-genome sequencing: identification of additional pathogenic variation across the genome.
作者信息
Mills James Dominic, Sisodiya Sanjay M
机构信息
Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
Chalfont Centre for Epilepsy, Buckinghamshire, UK.
出版信息
Brain Commun. 2021 Nov 19;3(4):fcab280. doi: 10.1093/braincomms/fcab280. eCollection 2021.
Abstract
This scientific commentary refers to ‘Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome’, by Qaiser et al. (https://doi.org/10.1093/braincomms/fcab207).
摘要
本科学评论参考了凯泽等人的《基因组测序鉴定Lennox-Gastaut综合征中的罕见串联重复扩增和拷贝数变异》（https://doi.org/10.1093/braincomms/fcab207）。
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